What is the (R)-(+)-1-Phenylethylamine?

(R)-(+)-1-Phenylethylamine is Colorless to light yellow liqui, while it's Molecular Formula is C8H11N. Colorless to light yellow liqui (R)-(+)-a-Methylbenzylamine also known as (R)-(+)-1-Phenylethylamine may be used in resolution of a chiral arylalkylamine involving high-conversion enantioselective condensation with capric acid followed by hydrolysis to yield corresponding (R)-(+)-amide.

What is the CAS number for (R)-(+)-1-Phenylethylamine?

The CAS number of (R)-(+)-1-Phenylethylamine is 3886-69-9.

What is (R)-(+)-1-Phenylethylamine (3886-69-9) used for?

(1R)-1-Phenylethanamine, also known as (R)-1-phenylethanamine, is an organic compound which is a primary amine. It's structure consists of a phenyl group attached to the ethylamine moiety, with the amine group (NH2) at the end of the ethyl chain.InChI:InChI=1/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/p+1/t7-/m1/s1

What is the (R)-(+)-1-Phenylethylamine?

(R)-(+)-1-Phenylethylamine is Colorless to light yellow liqui, while it's Molecular Formula is C8H11N. Colorless to light yellow liqui (R)-(+)-a-Methylbenzylamine also known as (R)-(+)-1-Phenylethylamine may be used in resolution of a chiral arylalkylamine involving high-conversion enantioselective condensation with capric acid followed by hydrolysis to yield corresponding (R)-(+)-amide.

What is the CAS number for (R)-(+)-1-Phenylethylamine?

The CAS number of (R)-(+)-1-Phenylethylamine is 3886-69-9.

What is (R)-(+)-1-Phenylethylamine (3886-69-9) used for?

(1R)-1-Phenylethanamine, also known as (R)-1-phenylethanamine, is an organic compound which is a primary amine. It's structure consists of a phenyl group attached to the ethylamine moiety, with the amine group (NH2) at the end of the ethyl chain.InChI:InChI=1/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/p+1/t7-/m1/s1

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(theta)-benzenemethanamin

Chemical raw materials, non-pharmaceuticals.
Product Name: (theta)-benzenemethanamin
CasNo: 3886-69-9
Purity:
Appearance: Colorless to light yellow liqui

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CasNo： 3886-69-9

Molecular Formula： C₈H₁₁N

Appearance： Colorless to light yellow liqui

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Molecular Formula:C8H11N
Molecular Weight:121.182
Appearance/Colour:Colorless to light yellow liqui
Vapor Pressure:0.5 mm Hg ( 20 °C)
Melting Point:-10 °C
Refractive Index:1.5260
Boiling Point:183 °C at 760 mmHg
PKA:9.04±0.10(Predicted)
Flash Point:75.8 °C
PSA：26.02000
Density:0.956 g/cm³
LogP:2.40660

(R)-(+)-1-Phenylethylamine(Cas 3886-69-9) Usage

Flammability and Explosibility	Nonflammable
Purification Methods	Dissolve the amine in toluene, dry over NaOH and distil; fraction boiling at 187-188o/atm is collected. Store it under N2 to avoid forming the carbamate and urea. Similarly for the S-(-) enantiomer [2627-86-3]. [Ingersoll Org Synth Coll Vol II 503 1943, Robinson & Snyder Org Synth Coll Vol III 717 1955, Beilstein 12 IV 2424, 2425.]
Categories	(1R)-1-Phenylethanamine belongs to the category of chiral amines and is commonly used in chiral resolutions.
Uses and Mechanism of Action	(1R)-1-Phenylethanamine is utilized in chiral resolutions, particularly in crystallization processes to obtain diastereomeric salts with excellent diastereoselectivity. In crystallization processes, (1R)-1-Phenylethanamine interacts with other compounds, such as cis-permethric acid, to form diastereomeric salts through specific intermolecular interactions, resulting in the separation of enantiomers.
Definition	ChEBI: The (R)-enantiomer of 1-phenylethanamine.
General Description	(R)-(+)-α-Methylbenzylamine is a chiral amine.

InChI:InChI=1/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/p+1/t7-/m1/s1

3886-69-9 Relevant articles

Synthesis and reactivity towards carbon monoxide of an optically active endo five-membered ortho-cyclopalladated imine: X-ray molecular structure of trans-(μ-Cl)2[Pd(κ2-C,N-(R)-C6H4-CH{double bond, long}N-CHMe-Ph)]2

Albert, Joan,D'Andrea, Luci?a,Granell, Jaume,Tavera, Raquel,Font-Bardia, Mercè,Solans, Xavier

, p. 3070 - 3080 (2007)

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Crystallization-based resolution of 1,4-benzodioxane-2-carboxylic acid enantiomers via diastereomeric 1-phenylethylamides

Fumagalli, Laura,Bolchi, Cristiano,Bavo, Francesco,Pallavicini, Marco

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Unlike the diastereomeric 1-phenylethyla...

Determination of absolute configurations of amines and amino acids using nonchiral derivatizing agents (NCDA) and deuterium NMR.

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Enantioselective Cascade Biocatalysis for Deracemization of Racemic β-Amino Alcohols to Enantiopure (S)-β-Amino Alcohols by Employing Cyclohexylamine Oxidase and ω-Transaminase

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Optically active β-amino alcohols are ve...

Highly Stable Zr(IV)-Based Metal-Organic Frameworks for Chiral Separation in Reversed-Phase Liquid Chromatography

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Separation of racemic mixtures is of gre...

Rational Design of Chiral Nanohelices from Self-Assembly of Meso-tetrakis (4-Carboxyphenyl) Porphyrin-Amino Acid Conjugates

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Generation of Oxidoreductases with Dual Alcohol Dehydrogenase and Amine Dehydrogenase Activity

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The l-lysine-?-dehydrogenase (LysEDH) fr...

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